Key result
Children with acute flaccid myelitis had more frequent asymmetric limb weakness (58% vs. 0%, p<0.001) and a shorter interval to nadir (3 vs. 8 days, p<0.001) compared to those with GBS.
Why the study?
Differentiation between acute flaccid myelitis and Guillain-Barré syndrome can be difficult, particularly in children.
What are the distinctive clinical features and diagnostic criteria specificities that differentiate acute flaccid myelitis from Guillain-Barré syndrome in children?
Cohort (n=182)
What are the distinctive clinical features and diagnostic criteria specificities that differentiate acute flaccid myelitis from Guillain-Barré syndrome in children?
Despite clinical overlap, AFM can be differentiated from GBS in children by early clinical features such as a shorter interval to nadir, asymmetric weakness, and lack of sensory deficits, alongside MRI and CSF findings.
This is the authors' abstract. We don't add key points for this paper.
BACKGROUND AND PURPOSE: Differentiation between acute flaccid myelitis (AFM) and Guillain-Barré syndrome (GBS) can be difficult, particularly in children. Our objective was to improve the diagnostic accuracy by giving recommendations based on a comparison of clinical features and diagnostic criteria in children with AFM or GBS. METHODS: A cohort of 26 children with AFM associated with enterovirus D68 was compared to a cohort of 156 children with GBS. The specificity of the Brighton criteria, used for GBS diagnosis, was evaluated in the AFM cohort and the specificity of the Centers for Disease Control and Prevention (CDC) AFM diagnostic criteria in the GBS cohort. RESULTS: Children with AFM compared to those with GBS had a shorter interval between onset of weakness and nadir (3 vs. 8 days, p < 0.001), more often had asymmetric limb weakness (58% vs. 0%, p < 0.001), and less frequently had sensory deficits (0% vs. 40%, p < 0.001). In AFM, cerebrospinal fluid leukocyte counts were higher, whereas protein concentrations were lower. Spinal cord lesions on magnetic resonance imaging were only found in AFM patients. No GBS case fulfilled CDC criteria for definite AFM. Of the AFM cases, 8% fulfilled the Brighton criteria for GBS, when omitting the criterion of excluding an alternate diagnosis. CONCLUSIONS: Despite the overlap in clinical presentation, we found distinctive early clinical and diagnostic characteristics for differentiating AFM from GBS in children. Diagnostic criteria for AFM and GBS usually perform well, but some AFM cases may fulfill clinical diagnostic criteria for GBS. This underlines the need to perform diagnostic tests early to exclude AFM in children suspected of atypical GBS.
Answers are grounded in this paper and cite their sources.
Early features may aid AFM vs GBS distinction in children; leaves open prospective validation with MRI/CSF criteria.
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Helfferich et al. (2021) conducted a cohort in Acute flaccid myelitis and Guillain-Barré syndrome (n=182). Acute flaccid myelitis vs. Guillain-Barré syndrome was evaluated on Asymmetric limb weakness (p=<0.001). Children with acute flaccid myelitis had more frequent asymmetric limb weakness (58% vs. 0%, p<0.001) and a shorter interval to nadir (3 vs. 8 days, p<0.001) compared to those with GBS.
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